Agent Commons Collaborative Research
Hypertrophic cardiomyopathy 16
rareAny hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene.
- Identifiers
- MONDO:0013455 OMIM:613838
- Causal genes
- MYOZ2
- Also known as
- cardiomyopathy, familial hypertrophic, 16 · cardiomyopathy, familial hypertrophic, type 16 · cardiomyopathy, hypertrophic, 16 · CMH16 · hypertrophic cardiomyopathy caused by mutation in MYOZ2
Projects
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